Extravirgin olive oil up-regulates CB1 tumor suppressor gene in human colon cancer cells and in rat colon via epigenetic mechanisms

被引:90
作者
Di Francesco, Andrea [1 ]
Falconi, Anastasia [1 ]
Di Germanio, Clara [2 ]
Di Bonaventura, Maria Vittoria Micioni [3 ]
Costa, Antonio [4 ]
Caramuta, Stefano [5 ,6 ]
Del Carlo, Michele [1 ]
Compagnone, Dario [1 ]
Dainese, Enrico [1 ,7 ]
Cifani, Carlo [3 ]
Maccarrone, Mauro [4 ,7 ]
D'Addario, Claudio [1 ,8 ]
机构
[1] Univ Teramo, Fac Biosci, Teramo, Italy
[2] Univ Teramo, Fac Vet Med, Teramo, Italy
[3] Univ Camerino, Sch Pharm, Pharmacol Unit, I-62032 Camerino, MC, Italy
[4] Univ Rome, Ctr Integrated Res, Campus Biomed, Rome, Italy
[5] Karolinska Inst, Dept Oncol Pathol, Stockholm, Sweden
[6] Karolinska Inst, Dept Mol Med & Surg, Stockholm, Sweden
[7] Santa Lucia Fdn IRCCS, European Ctr Brain Res, Rome, Italy
[8] Karolinska Inst, Dept Clin Neurosci, Stockholm, Sweden
关键词
Endocannabinoid system; Bioactive lipids; Colon; Epigenetics; Olive oil; Phenolic compounds; Hydroxytyrosol; MONOUNSATURATED FATTY-ACIDS; DNA METHYLATION; ENDOCANNABINOID SYSTEM; COLORECTAL-CANCER; HYDROXYTYROSOL; PREVENTION; EPIGENOME; CHEMOPREVENTION; CANNABINOIDS; ANANDAMIDE;
D O I
10.1016/j.jnutbio.2014.10.013
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Extravirgin olive oil (EVOO) represents the typical lipid source of the Mediterranean diet, an eating habit pattern that has been associated with a significant reduction of cancer risk. Diet is the more studied environmental factor in epigenetics, and many evidences suggest dysregulation of epigenetic pathways in cancer. The aim of our study was to investigate the effects of EVOO and its phenolic compounds on endocannabinoid system (ECS) gene expression via epigenetic regulation in both human colon cancer cells (Caco-2) and rats exposed to short- and long-term dietary EVOO. We observed a selective and transient up-regulation of CNR1 gene - encoding for type 1 cannabinoid receptor (CB1) - that was evoked by exposure of Caco-2 cells to EVOO (100 ppm), its phenolic extracts COPE, 50 mu M) or authentic hydroxytyrosol (HT, 50 mu M) for 24 h. None of the other major elements of the ECS (i.e., CB2; GPR55 and TRPV1 receptors; and NAPE-PLD, DAGL, FAAH and MAGL enzymes) was affected at any time point. The stimulatory effect of OPE and HT on CB, expression was inversely correlated to DNA methylation at CNR1 promoter and was associated with reduced proliferation of Caco-2 cells. Interestingly, CNR1 gene was less expressed in Caco-2 cells when compared to normal colon mucosa cells, and again this effect was associated with higher level of DNA methylation at CNR1. Moreover, in agreement with the in vitro studies, we also observed a remarkable (similar to 4-fold) and selective increase in CB1 expression in the colon of rats receiving dietary EVOO supplementation for 10 days. Consistently, CpG methylation of rat Cnr1 promoter, miR23a and miR-301a, previously shown to be involved in the pathogenesis of colorectal cancer and predicted to target CB1 mRNA, was reduced after EVOO administration down to similar to 50% of controls. Taken together, our findings demonstrating CB1 gene expression modulation by EVOO or its phenolic compounds via epigenetic mechanism, both in vitro and in vivo, may provide a new therapeutic avenue for treatment and/or prevention of colon cancer. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:250 / 258
页数:9
相关论文
共 52 条
[1]  
[Anonymous], 2007, Food, Nutrition, Physical Activity, and the Prevention of Cancer: a Global Perspective
[2]   Chemopreventive effect of the non-psychotropic phytocannabinoid cannabidiol on experimental colon cancer [J].
Aviello, Gabriella ;
Romano, Barbara ;
Borrelli, Francesca ;
Capasso, Raffaele ;
Gallo, Laura ;
Piscitelli, Fabiana ;
Di Marzo, Vincenzo ;
Izzo, Angelo A. .
JOURNAL OF MOLECULAR MEDICINE-JMM, 2012, 90 (08) :925-934
[3]   Epigenetic gene silencing in cancer - a mechanism for early oncogenic pathway addiction? [J].
Baylin, SB ;
Ohm, JE .
NATURE REVIEWS CANCER, 2006, 6 (02) :107-116
[4]   Targeting the endocannabinoid system in cancer therapy: A call for further research [J].
Bifulco, M ;
Di Marzo, V .
NATURE MEDICINE, 2002, 8 (06) :547-550
[5]  
Braga C, 1998, CANCER-AM CANCER SOC, V82, P448, DOI 10.1002/(SICI)1097-0142(19980201)82:3<448::AID-CNCR4>3.0.CO
[6]  
2-L
[7]   DNA Methylation of the First Exon Is Tightly Linked to Transcriptional Silencing [J].
Brenet, Fabienne ;
Moh, Michelle ;
Funk, Patricia ;
Feierstein, Erika ;
Viale, Agnes J. ;
Socci, Nicholas D. ;
Scandura, Joseph M. .
PLOS ONE, 2011, 6 (01)
[8]   Epigenetic mechanisms and endocannabinoid signalling [J].
D'Addario, Claudio ;
Di Francesco, Andrea ;
Pucci, Mariangela ;
Agro, Alessandro Finazzi ;
Maccarrone, Mauro .
FEBS JOURNAL, 2013, 280 (09) :1905-1917
[9]   Selective DNA Methylation of BDNF Promoter in Bipolar Disorder: Differences Among Patients with BDI and BDII [J].
D'Addario, Claudio ;
Dell'Osso, Bernardo ;
Palazzo, Maria Carlotta ;
Benatti, Beatrice ;
Lietti, Licia ;
Cattaneo, Elisabetta ;
Galimberti, Daniela ;
Fenoglio, Chiara ;
Cortini, Francesca ;
Scarpini, Elio ;
Arosio, Beatrice ;
Di Francesco, Andrea ;
Di Benedetto, Manuela ;
Romualdi, Patrizia ;
Candeletti, Sanzio ;
Mari, Daniela ;
Bergamaschini, Luigi ;
Bresolin, Nereo ;
Maccarrone, Mauro ;
Altamura, A. Carlo .
NEUROPSYCHOPHARMACOLOGY, 2012, 37 (07) :1647-1655
[10]   DNA methylation, cancer susceptibility, and nutrient interactions [J].
Davis, CD ;
Uthus, EO .
EXPERIMENTAL BIOLOGY AND MEDICINE, 2004, 229 (10) :988-995